Markevich A, Kurasch S, Lehtinen O, Reimer O, Feng X, Muellen K, Turchanin A, Khlobystov AN, Kaiser U, Besley E (2016)
Publication Type: Journal article
Publication year: 2016
Book Volume: 8
Pages Range: 2711-2719
Journal Issue: 5
DOI: 10.1039/c5nr07539d
The electron beam induced functionalization of graphene through the formation of covalent bonds between free radicals of polyaromatic molecules and CC bonds of pristine graphene surface has been explored using first principles calculations and high-resolution transmission electron microscopy. We show that the energetically strongest attachment of the radicals occurs along the armchair direction in graphene to carbon atoms residing in different graphene sub-lattices. The radicals tend to assume vertical position on graphene substrate irrespective of direction of the bonding and the initial configuration. The "standing up" molecules, covalently anchored to graphene, exhibit two types of oscillatory motion-bending and twisting-caused by the presence of acoustic phonons in graphene and dispersion attraction to the substrate. The theoretically derived mechanisms are confirmed by near atomic resolution imaging of individual perchlorocoronene (C
APA:
Markevich, A., Kurasch, S., Lehtinen, O., Reimer, O., Feng, X., Muellen, K.,... Besley, E. (2016). Electron beam controlled covalent attachment of small organic molecules to graphene. Nanoscale, 8(5), 2711-2719. https://doi.org/10.1039/c5nr07539d
MLA:
Markevich, Alexander, et al. "Electron beam controlled covalent attachment of small organic molecules to graphene." Nanoscale 8.5 (2016): 2711-2719.
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